What are the limits for uniformity dosage content for tablets and capsules
- 5 Answers
- 21182 Views
- Micro Labs, I also Faced
- E-Mail Answers
Answer Posted / robi
Acceptance value for 10 tablets is less than 15%
| Is This Answer Correct ? | 22 Yes | 1 No |
Post New Answer View All Answers
How to fix the sample conc. in Related substances test by HPLC?
when we talk about change in entropy we consider total entropy means of surround +entropy of system but when we talk about change in Gibss free energy we consider entropy of system.explain with reason.
what is difference between UV - VISIBLE MODEL NO like 1600,1601,1700 etc ? plz explain me
inhouse product is in capsule form in combination and RLD is in tablet form then can we proceed for multimedia CDP? in inhouse capsule product disso is paddle with sinker in release media is there then RLD product in tablet form then with same as paddle with sinker we can proceed n.a.?
in api coa contains only process impurities and in product coa contains degradation impurities?
How to set analytical specification for combination products?
why we use Dichlorobenzene.nitrobezine.t-butyldi sulhate.for calibration of gc Head space
Why irmoisture balance is used for corrugated box moisture testing
4. Describe the operation of the Craig apparatus. Chapter.3 Equilibrium Processes in Separations
For limit test of heavy metals in BP, Method C require that the substance is ignited at a temperature not exceeding 800 °C. Why confines such the temperature?
If combination product how require to identify which imp is of which api?
Why acetonitrile and water are used as extraction solvent when analysis melamine? I thought they are miscible and won't be able to separate...
What is the difference between spectro meter and spectro photo meter?
CAN WE DETERMINE THE PEAK PURITY IN GAS CHROMATOGRAPHY ANALYSIS?
which batch require to use for analytical method validation?
